NCT03512795 Optimization of HIV-1 DNA Genotyping by High Throughput Sequencing to Document Antiretroviral Resistant Mutations Status COMPLETED Phase N/A
NCT03512210 Monitoring SOF/VEL in Treatment Naïve, HCV Participants With Active Infection Status COMPLETED Phase PHASE4
NCT03493568 Switch From Dual Regimens Based on Dolutegravir Plus a Reverse Transcriptase Inhibitor to E/C/F/TAF in Virologically Suppressed, HIV-1 Infected Patients (Be-OnE) Status TERMINATED Phase PHASE3
NCT03472326 Study to Evaluate the Efficacy of GS-9131 Functional Monotherapy in Human Immunodeficiency Virus (HIV)-1-Infected Adults Failing a Nucleos(t)Ide Reverse Transcriptase Inhibitor-Containing Regimen With Nucleos(t)Ide Reverse Transcriptase Inhibitor Resistant Virus Status TERMINATED Phase PHASE2
NCT03416790 IMPAACT 2015 - Evaluation of the HIV-1 Reservoir in the Central Nervous System of Perinatally-Infected Youth and Young Adults With Cognitive Impairment Status COMPLETED Phase N/A
NCT03399903 Study of Pentasa® for Reducing Residual Systemic Immune Activation in Treated HIV Infection Status COMPLETED Phase PHASE1/PHASE2
NCT03392805 Infectious Diseases and Movement Program: Study of the Effects of Physical Activity on HIV Infection Status UNKNOWN Phase NA
NCT03360682 Clinical Trial to Evaluate the Efficacy, Pharmacokinetics (PK) Interactions and Safety of Dolutegravir Plus 2 Nucleoside Reverse Transcriptase Inhibitors (NRTIs) in HIV-1-Infected Solid Organ Transplant Patients Status COMPLETED Phase PHASE4
NCT03340077 The Medicines Optimisation Review Toolkit Evaluation in HIV Outpatients Status COMPLETED Phase NA
NCT03333083 Study With Dual Therapy Including Lamivudine (300 mg QD) Plus Raltegravir (1200 mg QD) in Virologically Suppressed HIV-1 Infected Patients Experiencing Inconvenience, Toxicity, Negative Impact on Co-morbidities or Risk of Drug-drug Interactions With Their Current Regimen Status TERMINATED Phase PHASE3
NCT03312244 Pyridostigmine as Immunomodulator in People Living With HIV Status SUSPENDED Phase PHASE2
NCT03311945 Simplification Study of HIV-1 Infected Patients With Virological Suppression Under the Combination of Lamivudine (150 mg BID) Plus Raltegravir (400 mg BID) Switching to Lamivudine (300 mg QD) Plus Raltegravir (1200 mg QD) : Roll-over Study of the RALAM Status COMPLETED Phase PHASE3